Canonical Allele Identifier: CA355975590
Gene: FGFR3 HGNC NCBI

Linked Data

dbSNP Id: rs1577275171

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.1801692G>T , CM000666.2:g.1801692G>T GRCh38
NC_000004.11:g.1803419G>T , CM000666.1:g.1803419G>T GRCh37
NC_000004.10:g.1773217G>T NCBI36
NG_012632.1:g.13381G>T , LRG_1021:g.13381G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000340107.9:c.688G>T ENSP00000339824.4:p.Val230Leu
ENST00000260795.8:c.688G>T ENSP00000260795.3:p.Val230Leu
ENST00000352904.6:c.688G>T ENSP00000231803.1:p.Val230Leu
ENST00000412135.7:c.676G>T ENSP00000412903.3:p.Val226Leu
ENST00000440486.8:c.688G>T MANE Select ENSP00000414914.2:p.Val230Leu
ENST00000481110.7:c.688G>T ENSP00000420533.2:p.Val230Leu
ENST00000260795.6:c.688G>T ENSP00000260795.2:p.Val230Leu
ENST00000340107.8:c.688G>T ENSP00000339824.4:p.Val230Leu
ENST00000352904.5:c.688G>T ENSP00000231803.1:p.Val230Leu
ENST00000412135.6:c.688G>T ENSP00000412903.2:p.Val230Leu
ENST00000440486.6:c.688G>T ENSP00000414914.2:p.Val230Leu
ENST00000474521.1:n.64G>T
ENST00000481110.6:c.688G>T ENSP00000420533.2:p.Val230Leu
ENST00000507588.1:c.148G>T ENSP00000427289.1:p.Val50Leu
ENST00000613647.4:c.688G>T ENSP00000479472.1:p.Val230Leu
NM_000142.4:c.688G>T , LRG_1021t1:c.688G>T NP_000133.1:p.Val230Leu
NM_001163213.1:c.688G>T , LRG_1021t2:c.688G>T NP_001156685.1:p.Val230Leu
NM_022965.3:c.688G>T NP_075254.1:p.Val230Leu
XM_006713868.1:c.688G>T XP_006713931.1:p.Val230Leu
XM_006713869.1:c.688G>T XP_006713932.1:p.Val230Leu
XM_006713870.1:c.688G>T XP_006713933.1:p.Val230Leu
XM_006713871.1:c.688G>T XP_006713934.1:p.Val230Leu
XM_006713872.1:c.688G>T XP_006713935.1:p.Val230Leu
XM_006713873.1:c.688G>T XP_006713936.1:p.Val230Leu
XM_011513420.1:c.688G>T XP_011511722.1:p.Val230Leu
XM_011513422.1:c.688G>T XP_011511724.1:p.Val230Leu
NM_001354809.1:c.688G>T NP_001341738.1:p.Val230Leu
NM_001354810.1:c.688G>T NP_001341739.1:p.Val230Leu
NR_148971.1:n.944G>T
NM_001354809.2:c.688G>T NP_001341738.1:p.Val230Leu
NM_001354810.2:c.688G>T NP_001341739.1:p.Val230Leu
NR_148971.2:n.963G>T
NM_000142.5:c.688G>T MANE Select NP_000133.1:p.Val230Leu
NM_001163213.2:c.688G>T NP_001156685.1:p.Val230Leu
NM_022965.4:c.688G>T NP_075254.1:p.Val230Leu